Gardner Syndrome

Alexandra Golant; Joshua A. Zeichner

doi:10.1007/978-1-4614-8344-1_29

Gardner Syndrome

Alexandra Golant, Joshua A. Zeichner

Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

2 Scopus citations

Abstract

Gardner syndrome (GS) is a phenotypic variant of familial adenomatous polyposis (FAP). The syndrome is characterized by premalignant intestinal polyposis and distinct extraintestinal features, such as multiple epidermoid cysts, osteomas, and desmoid or fibrous tumors of the skin and soft tissue [1].

Original language	English
Title of host publication	Acneiform Eruptions in Dermatology
Subtitle of host publication	A Differential Diagnosis
Publisher	Springer New York
Pages	201-206
Number of pages	6
ISBN (Electronic)	9781461483441
ISBN (Print)	9781461483434
DOIs	https://doi.org/10.1007/978-1-4614-8344-1_29
State	Published - 1 Jan 2014

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title = "Gardner Syndrome",

abstract = "Gardner syndrome (GS) is a phenotypic variant of familial adenomatous polyposis (FAP). The syndrome is characterized by premalignant intestinal polyposis and distinct extraintestinal features, such as multiple epidermoid cysts, osteomas, and desmoid or fibrous tumors of the skin and soft tissue [1].",

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AB - Gardner syndrome (GS) is a phenotypic variant of familial adenomatous polyposis (FAP). The syndrome is characterized by premalignant intestinal polyposis and distinct extraintestinal features, such as multiple epidermoid cysts, osteomas, and desmoid or fibrous tumors of the skin and soft tissue [1].

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BT - Acneiform Eruptions in Dermatology

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ER -

Gardner Syndrome

Abstract

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